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Gadolinium Ions Block Mechanosensitive Channels by Altering the Packing and Lateral Pressure of Anionic Lipids

机译:d离子通过改变阴离子脂质的堆积和侧向压力来阻断机械敏感通道

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摘要

Effects of polyvalent ions on the lateral packing of phospholipids have been known for decades, but the physiological consequences have not been systematically studied. Gd3+ is a relatively nonspecific agent that blocks mechano-gated channels with a variable affinity. In this study, we show that the large mechanosensitive channel MscL of Escherichia coli is effectively blocked by Gd3+ only when reconstituted with negatively charged phospholipids (e.g., PS). Taking this lead, we studied effects of Gd3+ on monolayers and unilamellar vesicles made of natural brain PS, DMPS, and its mixtures with DMPC. In monolayer experiments, we found that μM Gd3+ present in the subphase leads to ∼8% lateral compaction of brain PS (at 35 mN/m). Gd3+ more strongly shrinks and rigidifies DMPS films causing a spontaneous liquid expanded-to-compact transition to the limiting 40 Å2/mol. Pressure-area isotherms of uncharged DMPC were unaffected by Gd3+, and neutralization of DMPS surface by low pH did not produce strong compaction. Upshifts of surface potential isotherms of DMPS monolayers reflected changes in the diffuse double layer due to neutralization of headgroup charges by Gd3+, whereas the increased packing density produced up to a 200 mV change in the interfacial dipole potential. The slopes of surface potential versus reciprocal area predicted that Gd3+ induced a modest (∼18%) increase in the magnitude of the individual lipid dipoles in DMPS. Isothermal titration calorimetry indicated that binding of Gd3+ to DMPS liposomes in the gel state is endothermic, whereas binding to liquid crystalline liposomes produces heat consistent with the isothermal liquid-to-gel phase transition induced by the ion. Both titration curves suggested a Kb of ∼106 M−1. We conclude that anionic phospholipids serve as high-affinity receptors for Gd3+ ions, and the ion-induced compaction generates a lateral pressure increase estimated as tens of mN/m. This pressure can “squeeze” the channel and shift the equilibrium toward the closed state.
机译:数十年来人们已经知道多价离子对磷脂的横向堆积的影响,但尚未对生理后果进行系统的研究。 Gd3 +是一种相对非特异性的试剂,以可变的亲和力阻断机械门控通道。在这项研究中,我们表明,只有用带负电荷的磷脂(例如PS)重构后,大的机械敏感通道MscL才可以被Gd3 +有效地阻断。以此为主导,我们研究了Gd3 +对天然脑PS,DMPS及其与DMPC混合物制成的单层和单层囊泡的影响。在单层实验中,我们发现亚相中存在的μMGd3 +导致〜约8%的脑PS横向压实(在35 mN / m时)。 Gd3 +更强烈地收缩和硬化DMPS薄膜,导致自发的液体膨胀至致密过渡到极限40Å2/ mol。不带电DMPC的压力-等温线不受Gd3 +的影响,低pH中和DMPS表面不会产生强压实。 DMPS单层的表面电势等温线的上移反映了由于Gd3 +中和头基电荷而中和了扩散双层的变化,而堆积密度的增加导致界面偶极电势变化高达200 mV。表面电势相对于倒数的斜率表明,Gd3 +引起DMPS中单个脂质偶极子幅度的适度增加(〜18%)。等温滴定量热法表明,凝胶状态下Gd3 +与DMPS脂质体的结合是吸热的,而与液晶脂质体的结合产生的热量与离子诱导的等温液体-凝胶相变一致。两条滴定曲线均表明Kb约为106 M-1。我们得出的结论是,阴离子磷脂可作为Gd3 +离子的高亲和力受体,并且离子诱导的压实会产生估计为数十mN / m的侧向压力增加。该压力可以“挤压”通道并使平衡向闭合状态移动。

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